Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.47332122G>CCA221681757MYBPC3c.3764C>G (p.Ala1255Gly)
c.3746C>G (p.Ala1249Gly)
c.3683C>G (p.Ala1228Gly)
ClinVar dbSNP gnomAD v4
11g.47332122G>TCA014820MYBPC3c.3764C>A (p.Ala1255Asp)
c.3746C>A (p.Ala1249Asp)
c.3683C>A (p.Ala1228Asp)
ClinVar dbSNP

Number of alleles fetched